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"Andoro" abdominal aortic aneurysm stent delivery therapy system - Taiwan Registration bf4225080e276309ab60601b502dad54

Access comprehensive regulatory information for "Andoro" abdominal aortic aneurysm stent delivery therapy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bf4225080e276309ab60601b502dad54 and manufactured by Endologix International Holdings B.V;; Endologix, Inc.. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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bf4225080e276309ab60601b502dad54
Registration Details
Taiwan FDA Registration: bf4225080e276309ab60601b502dad54
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Device Details

"Andoro" abdominal aortic aneurysm stent delivery therapy system
TW: โ€œๅฎ‰ๅคš็พ…โ€่…นไธปๅ‹•่„ˆ็˜คๆ”ฏๆžถๆšจ่ผธ้€ๆฒป็™‚็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

bf4225080e276309ab60601b502dad54

DHA05603161309

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.0006.

The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Jun 21, 2019

Jun 21, 2024

Dec 18, 2020

Cancellation Information

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